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Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome

โœ Scribed by Toshiyuki Yamamoto; Kiyoko Sameshima; Ken-ichi Sekido; Noriko Aida; Naomichi Matsumoto; Kenji Naritomi; Kenji Kurosawa

Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
106 KB
Volume
140A
Category
Article
ISSN
1552-4825

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This report is on a 14-month-old boy with manifestations of Opitz (G/BBB) syndrome in whom a 22q11.2 deletion was found. Deletion analysis was requested because of some findings in this patient reminiscent of velocardiofacial (VCF) syndrome. The extent of aspiration and of respiratory symptoms in th

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Genetic syndromes associated with deletions at chromosome 22q11 generally have been diagnosed during childhood based on a constellation of physical features. To investigate a reported association of velocardiofacial syndrome with psychotic disorders in adults, we assessed subjects with DSM-IV schizo